cDNA of DOCK180 gene and DOCK180 protein
The present invention provides a cDNA of DOCK180 gene, which has a nucleotide sequence of SEQ ID NO: 1 and of which translation product binds to the proto-oncogene product CRK, a recombinant vector containing this cDNA, a DOCK180 protein expressed from the EDNA which has a amino acid sequence of SEQ ID NO: 2, and an antibody to the DOCK180 protein. According to the present invention, It is possible to develop new diagnosing and therapeutic techniques using DOCK180 protein and antibody against the protein.
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1. Field of the Invention
The present invention relates to a cDNA of DOCK180 protein, which binds to the proto-oncogene product CRK, a recombinant vector containing this cDNA, a DOCK180 protein expressed from the cDNA, and an antibody to the DOCK180 protein. The cDNA of the present invention, the DOCK180 protein, and the antibody are very useful for diagnosis of tumor cells and development of a cancerocidal method for suppressing tumor cells.
2. Description of Related Art
Recent progress of cellular biology and molecular biology is really remarkable. Active research efforts are being made on carcinogenesis on the genetic level, and such efforts have identified many oncogenes and antioncogenes associated with human. It is also known that various proteins are expressed from these genes.
For example, CRK protein, which is expressed from a proto-oncogene CRK, is one of the major proteins controlling proliferation of higher eukaryote, and is known to regulate proliferation of tumor cells in many malignant tumors.
It has now been revealed that this CRK protein functions through binding to DOCK180 protein. DOCK180 is therefore attracting attention as a diagnostic indicator of tumor cells and as a target for missile therapy using various antitumor agents.
However, because no information has been available about a gene encoding the DOCK180 protein, it has been impossible to effectively utilize this protein widely for diagnosis of cancerous diseases, clarification of carcinogenesis mechanism, or development or a new cancer therapy.
SUMMARY OF THE INVENTIONThe present invention has an object to provide a cDNA of DOCK 180 gene and a genotic engineering material permitting easy manipulation of this cDNA and expression of the protein in a large scale.
The present invention has another object to provide a DOCK180 protein which is expressed from the above-mentioned cDNA, and an antibodies against this protein.
The present invention provides a cDNA of the DOCK180 gene, which has the nucleotide sequence defined in Sequence Listing by SEQ ID NO: 1.
Furthermore, the present invention provides a recombinant vector containing the cDNA of DOCK180 gene. More concretely, the present invention provides the plasmid pDOCK180 held by E. coli DOCK180 (FERM BP-5362).
The present invention further provides a DOCK180 protein having the amino acid sequence defined in Sequence Listing by SEQ ID NO: 2, and antibodies to DOCK180 protein prepared by using the DOCK180 protein as an antigen.
BRIEF DESCRIPTION OF THE DRAWINGFIG. 1 is a constitutional diagram of pDOCK180, which is a cloning vector of the present invention.
DETAILED DESCRIPTION OF THE INVENTIONThe cDNA of the present invention can be isolated and purified from higher eukaryotes such as cells derived from human, mouse, and chicken by the application of, for example, the method of Sambrook et al.(Molecular Cloning, second edition, Cold Spring Harbor Laboratory, New York, 1989). More specifically, the cDNA can be obtained by purifying mRNA of DOCK180 protein gene from animal cell, and then synthesizing a cDNA chain from the mRNA by the use of reverse transcriptase. From among the thus synthesizable cDNAs of DOCK180 protein, the nucleotide sequence of cDNA derived from human cells and the amino acid sequence of the translation domain thereof are defined in Sequence Listing by SEQ ID NOs: 1 and 2.
Then, the recombinant vector of the present invention can be prepared by inserting a fragment of the resultant cDNA into known cloning vectors. Ligation of the cDNA fragments and the vectors may be accomplished by, for example, the above-mentioned method of Sambrook et al. Preferable vectors include a plasmid and a .lambda.-phage for Escherichia coli as the host, and an applicable plasmid is, for example, one derived from pBR322. A preferable .lambda.-phase is .lambda. gt11.
Transfer of the thus prepared recombinant vectors into the host may be conducted through infection by .lambda.-phage as presented in the above-mentioned paper by Sambrook et al. For example, a transformed cells with the recombinant vector containing the above-mentioned cDNA are available by inoculating the recombinant .lambda. gt11 into Escherichia coli Y1090 at 37.degree. C.
Selection of a transformed cell may be accomplished by using a known method, depending upon the kind of the cloning vector. For example, selection of a transformed cell with .lambda. gt11 can be performed as follows. The above-mentioned recombinant .lambda. gt11 containing the cDNA can be inoculated into Escherichia coli Y1090 under a temperature condition of 37.degree. C., and the E. coli cells are cultured on an ager plate containing trypton, yeast extract, NaCl and ampicillin (hereinafter abbreviated as an "agar medium"). Then, a nitrocellulose membrane containing isopropyl thio-D-galactoside (hereinafter abbreviated as "IPTG") is placed on the plate for another several hours to induce transcription from the integrated cDNA. After the binding of an enzyme-labelled CRK protein to the membrane (Matsuda et al., Mol. Cell. Biol., 12: 3482-3489, 1992), an lamda phase plaques having the recombinant vector can be selected by putting a substrate for the enzyme in it. A preferable labelling enzyme is alkaline phosphatase or peroxidase. CRK protein may be manufactured as a fusion protein with glutathione S-transferese (hereinafter abbreviated as "GST"), and selection may be accomplished by using an antibody against this GST.
The cDNA fragment inserted into .lambda. phage can be cleaved out and re-inserted into a plasmid vector, if necessary. An example or recombinant plasmid vector of the invention is pDOCK180 which is prepared by inserting the cDNA of SEQ ID NO: 1 into vector plasmid pBlue ScriptIIKS(+), for which details are presented in Example 2 later. The pDOCK180 was transfected into the XL1-Blue strain derived from Escherichia coli K12 strain, and the transformant E. coli DOCK180 having the pDOCK180 was deposited to National Institute of Biocience and human Technology, an international depository, under Budapest Treaty as a deposit No. FERM BP-5362 on Jan. 12, 1996.
Then, the DOCK180 protein of the present invention can be exressed from the cDNA of SEQ ID NO: 1. For production of the protein, an expression vector is prepared by inserting the cDNA fragment into a known expression vector. The cDNA fragment can be isolated from the above-mentioned cloning vector, pDOCK180. While there is no particular limitation as to the expression vector, a preferable one is pGEX1, pG5X2T or pGEX3X using E. coli as the host. The expression vector containing the cDNA fragment can be introduced into an Escherichia coli (for example, DH5 strain derived from Escherichia coli K12 strain) by a known method. The DOCK180 protein of the present invention is easily produced in a large scale by culturing the transformed cells. More specifically, a concrete example comprises the stops of culturing the transformed Escherichia coli at 37.degree. C. for 3 to 24 hours on L-broth containing ampicillin, bacteriolyzing through ultrasonic blending, and adsorbing this sample to a carrier such as glutathione sephalose (made by Pharmacia P-L Biochemicals Company), thereby isolating and purifying the target DOCK180 protein.
An antibody against DOCK180 protein is available by inoculating the thus purified DOCK180 protein to an animal by a conventional method. Applicable animals include rabbit, mouse, goat, sheep, horse and hamster, and among others, rabbit or mouse is preferable.
The thus obtained anti-DOCK180 protein antibody can be used, for example, for quantitative determination or separation of DOCK180 protein in a sample, and further, serves as a useful material for missile therapy using an antitumor agent with DOCK180 as a target.
The cDNA, the protein and the antibody of the present invention provide various genetic manipulation materials useful for development of a new cancer therapy. These materials include an antisense RNA of DOCK180 gene, a variant protein of DOCK180, and a virus vector which expresses these RNA, variant protein, and anti-DOCK180 protein antibody in tumor cells.
The present invention will be described below in further detail by means of examples. It is needless to mention that the present invention Is not limited in any manner by the following examples.
EXAMPLE 1A cDNA fragment to human DOCK180 protein gene was isolated and cloned as follows.
An mRNA of DOCK180 gene was isolated from human spleen and a cDNA fragment was synthesized from the mRNA. The cDNA fragment was then integrated into .lambda. gt11, and a recombinant vector thereof was infected to Escherichia coli Y1090, which was plated onto LA agar culture medium. After six hours, a nitrocellulose membrane containing 1 mM IPTG was placed on this medium, and after three hours of culture, this nitrocellulose membrane was Incubated for an hour with a phosphate buffer solution (pH: 7.5) containing 2% skim milk and 0.05% Tween 20. Then, after reaction for an hour with a phosphate buffer solution containing 1 .mu.g/ml GST-CRK and 1 .mu.g/ml anti-GST monoclonal antibody, and for an hour with 1 .mu.g/ml alkaline phosphate-labelled anti-mouse antibody (made by TAGO Company), the phage having an ability to bind to CRK protein was identified by means of AP PURPLE (made by Bio Iol Company), a substrate for alkaline phosphatase. This phage was purified through three runs of plaque formation, and then DNA thereof was isolated by the phenol extraction method, and cleaved with a restriction enzyme EcoRI. Next, part of cDNA of DOCK180 gene was prepared through electrophoresis. This cDNA fragment was isotope-labelled with random oligo primer (made by Behlinger Company) and 32P-deoxycytidine triphosphate. With the use of this labelled cDNA, the above-mentioned recombinant .lambda. gt11 with cDNA derived from a human spleen was screened through plaque hybridization by the method of Sambrook et al. (Molecular Cloning, second edition, Cold Spring Harbor Laboratory, New York, 1989), and further six clones of recombinant .lambda. gt11 having DOCK180 protein cDNA were obtained. DNAs of these phages were cleaced with restriction enzyme EcoRI to isolate cDNA of DOCK180 gene and subcloned into phagemid vector pUC119. A single stranded DNA was purified from the thus obtained recombinant vector, and the nucleotide sequence thereof was determined by the use of an automatic nucleotide sequence reader (made by ABI Company). The identified nucleotide sequence thereof is shown in Sequence Listing by SEQ ID NO; 1, and the amino acid sequence of the anticipated translation product, by SEQ ID NO: 2. As a result of retrieval of this amino acid sequence in the database in the GenBank of the European Molecular Biology Laboratories (EMBL), the amino terminal end of DOCK180 protein shares homology with Fyn and Yes of tyrosine kinase by more than 20%. This domain has a structure known as SH3, and is present in various protein groups involved in signal transduction of cell proliferation in addition to that of tyrosine kinase. However, DOCK180 protein was found to be different from any known proteins and to be a new signal transduction factor.
EXAMPLE 2From the group of recombinant pUC119 obtained in Example 1, the DNA fragments excluding overlapping portions were isolated and ligated each other to prepare a fragment containing all the translation domain of the cDNA. The resultant cDNA fragment was then inserted into the plasmid vector pBlue Script II KS(+) to obtain the recombinant vector pDOCK180. This pDOCK180 has a constitution as shown In FIG. 1.
Further, this cloning vector pDOCK180 was introduced into an XL1-Blue strain derived from Escherichia coli K12 to obtain a transformant E. coli DOCK180 (FERM BP-5362).
EXAMPLE 3The cloning vector pDOCK180 obtained by Example 2 was cleaved with a restriction enzyme to prepare a cDNA domain of DOCK180 protein. The resultant cDNA fragment was then inserted into plasmid pGEX1, thereby preparing expression vectors. Transformant cells were prepared by introducing the expression vectors into Escherichia coli DH5. After culturing this transformant cells in 1 l L-broth containing ampicillin up to an absorbance of 0.6, IPTG was added to 0.5 mM, and culturing was continued for another three hours. After collection, the bacteria were ultrasonic-treated to remove crushed pieces of bacteria, and the supernatant was mixed with glutathione sephalose (made by Pharmacia P-L Biochemicals Company). After rinsing glutathione sephalose with a phosphate buffer solution, DOCK180 protein was eluded with the use of a phosphate buffer solution containing 5 mM glutathione. This protein was dialyzed with a phosphate buffer solution, and then a portion thereof was analyzed with SDS-polyacrylamide gel: a GST fused-DOCK180 protein having a purity of over 90% was synthesized.
EXAMPLE 4The DOCK180 protein purified in Example 3 was subcutaneously inoculated three times to a rabbit, together with complete Freund's adjuvant, and then, serum was sampled.
Reactivity of this serum with the purified DOCK180 protein was investigated by the Western blotting technique: a clear reactivity was demonstrated with the DOCK180 protein even when diluted to about 1,000. This permitted confirmation of applicability thereof as an antibody against DOCK180 protein.
__________________________________________________________________________ SEQUENCE LISTING (1) GENERAL INFORMATION: (iii) NUMBER OF SEQUENCES: 2 (2) INFORMATION FOR SEQ ID NO:1: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 6519 base pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA to mRNA (iii) HYPOTHETICAL: (iv) ANTI-SENSE: (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE: spleen cell of homo sapiens (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 24..5619 (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1: GCACGAGCGGCTCCGGCGGCGCCATGACGCGCTGGGTGCCCACCAAGCGCGAGGAGAAGT60 ACGGCGTGGCTTTTTATAACTATGATGCCAGAGGAGCGGATGAACTTTCTTTACAGATCG120 GAGACACTGTGCACATCTTAGAAACATATGAAGGGTGGTACCGAGGTTACACGTTACGAA180 AAAAGTCTAAGAAGGGTATATTTCCTGCTTCATATATTCATCTTAAAGAAGCGATAGTTG240 AAGGAAAAGGGCAACATGAAACAGTCATCCCGGGTGACCTCCCCCTCATCCAGGAAGTCA300 CCACGACACTCCGAGAGTGGTCCACCATCTGGAGGCAGCTCTACGTGCAAGATAACAGGG360 AGATGTTTCGAAGTGTGCGGCACATGATCTATGACCTTATTGAATGGCGATCACAAATTC420 TTTCTGGAACTCTGCCTCAGGATGAACTCAAAGAACTGAAGAAGAAGGTCACAGCCAAAA480 TTGATTATGGAAACAGAATTCTAGATTTGGACCTGGTGGTTAGAGATGAAGATGGGAATA540 TTTTGGATCCAGAATTAACTAGCACGATTAGTCTCTTCAGAGCTCATGAAATAGCTTCTA600 AACAAGTGGAGGAAAGGTTACAAGAGGAAAAATCTCAAAAGCAGAACATAGATATTAACA660 GACAAGCCAAGTTTGCTGCAACCCCTTCTCTGGCCTTGTTTGTGAACCTCAAAAATGTGG720 TTTGTAAAATAGGAGAAGATGCTGAAGTCCTCATGTCTCTATATGACCCTGTGGAGTCCA780 AATTCATCAGTGAGAACTACCTGGTTCGCTGGTCCAGTTCAGGATTACCTAAAGACATAG840 ACAGATTACATAATTTGCGAGCCGTGTTTACTGACCTCGGAAGCAAAGACCTGAAAAGGG900 AGAAAATCAGTTTTGTCTGTCAGATTGTTCGCGTGGGTCGCATGGAGCTGAGGGACAACA960 ACACCAGGAAACTGACCTCGGGGTTGCGGCGACCTTTTGGAGTGGCTGTGATGGATGTAA1020 CAGATATAATAAATGGAAAAGTAGATGATGAAGATAAGCAGCATTTCATTCCCTTTCAGC1080 CGGTGGCAGGGGAGAATGACTTCCTTCAGACTGTTATAAACAAAGTCATCGCTGCCAAAG1140 AAGTCAACCACAAGGGGCAGGGTTTGTGGGTAACATTGAAATTACTTCCTGGAGATATCC1200 ATCAGATCCGAAAAGAGTTTCCGCATTTAGTGGACAGGACCACAGCTGTGGCTCGAAAAA1260 CAGGGTTTCCGGAGATAATCATGCCTGGTGATGTTCGAAATGATATCTATGTAACATTAG1320 TTCAAGGAGATTTTGATAAAGGAAGCAAAACAACAGCGAAGAACGTGGAGGTCACGGTGT1380 CTGTGTACGATGAGGATGGGAAACGATTAGAGCATGTGATTTTCCCGGGTGCTGGTGATG1440 AAGCGATTTCAGAGTACAAATCTGTGATTTACTACCAAGTAAAGCAGCCACGCTGGTTTG1500 AGACTGTTAAGGTGGCCATTCCCATCGAGGACGTTAACCGCAGTCACCTTCGGTTTACCT1560 TCCGCCACAGGTCATCACAGGACTCTAAGGATAAATCTGAGAAAATATTTGCACTAGCAT1620 TTGTCAAGCTGATGAGATACGATGGTACCACCCTGCGAGACGGAGAGCACGATCTTATCG1680 TCTATAAGGCCGAAGCGAAGAAGCTGGAAGATGCTGCCACGTACTTGAGTCTGCCCTCCA1740 CGAAGGCAGAGTTGGAAGAAAAGGGCCACTCGGCCACCGGCAAGAGCATGCAGAGCCTTG1800 GGAGCTGCACCATTAGCAAGGACTCCTTCCAGATCTCCACGCTCGTGTGCTCCACCAAAC1860 TGACTCAGAACGTGGACCTTCTGGGGCTCTTGAAATGGCGCTCCAACACCAGCCTGCTGC1920 AGCAGAACTTGAGGCAGCTGATGAAAGTCGATGGTGGTGAAGTAGTGAAGTTTCTTCAGG1980 ACACGTTGGATGCCCTCTTCAACATCATGATGGAGAACTCAGAGAGTGAGACTTTTGACA2040 CGTTAGTCTTTGATGCTCTGGTATTTATCATTGGACTGATTGCTGATAGAAAATTTCAGC2100 ATTTTAATCCTGTTTTGGAAACTTACATTAAGAAACACTTTAGTGCAACGTTAGCCTACA2160 CGAAGTTGACAAAAGTGTTGAAGAACTACGTGGACGGTGCTGAGAAGCCGGGAGTAAATG2220 AGCAGCTGTACAAAGCCATGAAAGCGCTAGAATCCATCTTCAAGTTCATCGTGCGCTCCA2280 GGATCCTGTTCAATCAACTGTATGAAAACAAGGGAGAGGCTGACTTCGTGGAATCTTTGC2340 TGCAGCTCTTCAGGTCCATCAATGACATGATGAGCAGCATGTCAGACCAGACCGTCCGGG2400 TGAAGGGGGCAGCACTGAAATACTTACCAACGATCGTCAACGATGTGAAATTGGTGTTTG2460 ATCCCAAAGAGCTCAGCAAAATGTTTACTGAATTCATCCTCAATGTTCCCATGGGCTTGC2520 TGACCATCCAGAAACTCTACTGCTTGATCGAAATCGTCCACAGTGACCTCTTCACACAGC2580 ATGACTGCAGAGAGATCCTGCTTCCCATGATGACCGATCAGCTCAAGTACCATCTGGAGA2640 GACAGGAGGACCTGGAGGCCTGCTGTCAGCTGCTCAGCCACATCCTGGAGGTGCTGTACA2700 GGAAGGACGTGGGGCCAACCCAGAGGCACGTCCAGATTATCATGGAGAAACTTCTCCGGA2760 CCGTGAACCGAACCGTCATTTCCATGGGACGAGATTCTGAACTCATTGGAAACTTCGTGG2820 CTTGCATGACAGCTATTTTACGACAAATGGAAGATTACCATTATGCCCACTTGATCAAGA2880 CTTTTGGGAAAATGAGGACTGATGTGGTAGATTTCCTAATGGAAACATTCATCATGTTTA2940 AGAACCTCATTGGAAAGAACGTTTACCCCTTCGACTGGGTGATCATGAACATGGTGCAAA3000 ATAAAGTCTTCCTGCGAGCAATTAATCAGTATGCAGATATGCTGAACAAAAAATTTCTGG3060 ATCAAGCCAACTTTGAGCTACAGCTGTGGAACAACTACTTTCACCTGGCTGTTGCTTTCC3120 TTACTCAAGAGTCCCTGCAACTGGAGAATTTTTCAAGTGCCAAGAGAGCCAAAATCCTTA3180 ACAAGTACGGAGATATGAGGAGACAGATTGGCTTTGAAATCAGAGACATGTGGTACAACC3240 TTGGTCAACACAAGATAAAGTTCATTCCAGAAATGGTGGGCCCAATATTAGAAATGACAT3300 TAATTCCCGAGACGGAGCTGCGCAAAGCCACCATCCCCATCTTCTTTGATATGATGCAGT3360 GTGAATTCCATTCGACCCGAAGCTTCCAAATGTTTGAAAATGAGATCATCACCAAGCTGG3420 ATCATGAAGTCGAAGGAGGCAGAGGAGACGAACAGTACAAAGTGTTATTTGATAAAATCC3480 TTCTGGAACACTGCAGGAAGCACAAATACCTCGCCAAAACAGGAGAAACTTTTGTAAAAC3540 TCGTTGTGCGCTTAATGGAAAGGCTTTTGGATTATAGAACCATCATGCACGACGAGAACA3600 AAGAAAACCGCATGAGCTGCACCGTCAATGTGCTGAATTTCTACAAAGAAATTGAAAGAG3660 AAGAAATGTATATAAGGTATTTGTACAAGCTCTGTGACCTGCACAAGGAGTGTGATAACT3720 ACACCGAAGCGGCTTACACCTTGCTTCTCCATGCAAAGCTTCTTAAGTGGTCGGAGGATG3780 TGTGTGTGGCCCACCTCACCCAGCGGGACGGGTACCAGGCCACCACGCAGGGACAGCTGA3840 AGGAGCAGCTCTACCAGGAAATCATCCACTACTTCGACAAAGGCAAGATGTGGGAGGAGG3900 CCATTGCCTTGGGCAAGGAGCTAGCCGAGCAGTATGAGAACGAAATGTTTGATTATGAGC3960 AACTCAGCGAATTGCTGAAAAAACAGGCTCAGTTTTATGAAAACATCGTCAAAGTGATCA4020 GGCCCAAGCCTGACTATTTTGCTGTTGGCTACTACGGACAAGGGTTCCCCACATTCCTGC4080 GGGGAAAAGTTTTCATTTACCGAGGGAAAGAGTATGAGCCCCGGGAAGATTTTGAGGCTC4140 GGCTCTTAACTCAGTTTCCAAACGCCGAGAAAATGAAGACAACATCTCCACCAGGCGACG4200 ATATTAAAAACTCTCCTGGCCAGTATATTCAGTGCTTCACAGTGAAGCCCAAACTCGATC4260 TGCCTCCTAAGTTTCACAGGCCAGTGTCAGAGCAGATTGTAAGTTTTTACAGGGTGAACG4320 AGGTCCAGCGATTTGAATATTCTCGGCCAATCCGGAAGGGAGAGAAAAACCCAGACAATG4380 AATTTGCGAATATGTGGATCGAGAGAACCATATATACAACTGCATATAAATTACCTGGAA4440 TTTTAAGGTGGTTTGAGGTCAAGTCTGTTTTCATGGTGGAAATCAGCCCCCTGGAGAATG4500 CCATCGAGACCATGCAGCTGACGAACGACAAGATCAACAGCATGGTGCAGCAGCACCTGG4560 ATGACCCCAGCCTGCCCATCAACCCGCTCTCCATGCTCCTGAACGGCATCGTGGACCCAG4620 CTGTCATGGGGGGCTTCGCAAACTACGAAAAGGCCTTCTTTACAGACCGGTACCTGCAGG4680 AGCACCCTGAGGCCCATGAAAAGATCGAGAAGCTCAAGGACCTGATTGCTTGGCAGATTC4740 CTTTTCTGGCCGAAGGGATCAGAATCCATGGAGACAAAGTCACGGAGGCACTGAGGCCGT4800 TCCACGAGAGGATGGAGGCCTGTTTCAAACAGCTGAAGGAAAAGGTGGAGAAAGAGTACG4860 GCGTCCGAATCATGCCCTCAAGTCTGGATGATAGAAGAGGCAGCCGCCCCCGGTCCATGG4920 TGCGGTCCTTCACGATGCCTTCCTCATCCCGCCCTCTGTCTGTGGCCTCTGTCTCTTCCC4980 TCTCATCGGACAGCACCCCCTCCAGACCAGGCTCCGACGGGTTTGCCCTGGAGCCTCTCC5040 TGCCAAAGAAAATGCACTCCAGGTCCCAGGACAAGCTGGACAAGGATGACCTGGAGAAGG5100 AGAAGAAGGACAAGAAGAAGGAAAAAAGGAACAGCAAACATCAAGAGATATTTGAGAAAG5160 AATTTAAACCCACCGACATTTCCCTGCAGCAGTCTGAGGCTGTGATCCTTTCGGAAACGA5220 TAAGTCCCCTGCGGCCCCAGAGACCGAAGAGCCAGGTGATGAACGTCATTGGAAGCGAAA5280 GGCGCTTCTCGGTGTCCCCCTCGTCACCGTCCTCCCAGCAAACACCCCCTCCAGTTACAC5340 CAAGAGCCAAGCTCAGCTTCAGCATGCAGTCGAGCTTGGAGCTGAACGGCATGACGGGGG5400 CGGACGTGGCCGATGTCCCACCCCCTCTGCCTCTCAAAGGCAGCGTGGCAGATTACGGGA5460 ATTTGATGGAAAACCAGGACTTGCTGGGCTCGCCAACACCTCCACCTCCCCCTCCACACC5520 AGAGGCATCTGCCACCTCCACTGCCCAGCAAAACTCCGCCTCCTCCCCCTCCAAAGACAA5580 CTCGCAAGCAGACATCGGTGGACTCTGGGATCGTGCAGTGACATCGCAAGGCTCTCTGGA5640 AAGAGTGTGCTGCCCCTCCCCATCTCCATGCCCTCTCCTTCTGTGTCCCCTGAGTCTGCT5700 GTTTACCTCATTGGGCCTGTGATGTTAACATTTCGTGCGACTGCTTTTTCTTCAAAGGAG5760 TTCAGTTCTCACCATGGAGTGAGTGGCCTTTAGCGTCATGGAGCAAGGTGGGTCTGGGAG5820 GTAGATATGGGTCCGGGATGTGCCATCGTAGTTACCAGAGTTGGGGGCCTCTGAGTGTGT5880 CTGGCTCTGAGAGAGTCTGAGTCTTGCCCAAACATTCTTTCTTTTTGTGCCAAATGACTT5940 GCATTTGCAAAGAGCTCAATTGCTCTGAGCTCAGCCAAGTAGGAGAGGCTAGGCCATCAC6000 TCTTGGGAAGCTGTGTAGTGATGATGTATAAGAATCCTCCTCACTGTCATGGGATGTTGT6060 ATCCAGCCCCTCCTTGTTCCAGCCGGTGGTGTGACTTCGTTGGTTGAGGTGTGTCTCCAA6120 CCTACATCAGACCATGAAGTTCAACCCCTCCAGGGAAGCTCCTGATTTCCCCTGCATAAT6180 TGAAAATAGGATATTCTCAGCTATTGAACAGTTACTAATTTATGGGGTGGAAACAGCATT6240 AAGAATACTGAATCAAATGGAAAAACAAATGAATACAGGAAGATAAGTGTTCGTTCTTTT6300 CTGAAAAAAGAGTATGTGTACCACAAGAGCTGGTTTTAATTGGGTGAATTGTTTTTGTCC6360 TCATTCTGTACAGAAATTTGTATATATGATGGTTCTTAGAACTTGTTTTAATTTTTGTGG6420 TCCTTCTGTTTATTATAATAGGCGTCCACCAATGATTATCCATATGTGTTCTTAATTTTT6480 AACTGCTGGAAGTGTTAAAACACACACACCCCGGAATTC6519 (2) INFORMATION FOR SEQ ID NO:2: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1865 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: protein (iii) HYPOTHETICAL: (iv) ANTI-SENSE: (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE: spleen cell of homo sapiens (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2: MetThrArgTrpValProThrLysArgGluGluLysTyrGlyValAla 51015 PheTyrAsnTyrAspAlaArgGlyAlaAspGluLeuSerLeuGlnIle 202530 GlyAspThrValHisIleLeuGluThrTyrGluGlyTrpTyrArgGly 354045 TyrThrLeuArgLysLysSerLysLysGlyIlePheProAlaSerTyr 505560 IleHisLeuLysGluAlaIleValGluGlyLysGlyGlnHisGluThr 65707580 ValIleProGlyAspLeuProLeuIleGlnGluValThrThrThrLeu 859095 ArgGluTrpSerThrIleTrpArgGlnLeuTyrValGlnAspAsnArg 100105110 GluMetPheArgSerValArgHisMetIleTyrAspLeuIleGluTrp 115120125 ArgSerGlnIleLeuSerGlyThrLeuProGlnAspGluLeuLysGlu 130135140 LeuLysLysLysValThrAlaLysIleAspTyrGlyAsnArgIleLeu 145150155160 AspLeuAspLeuValValArgAspGluAspGlyAsnIleLeuAspPro 165170175 GluLeuThrSerThrIleSerLeuPheArgAlaHisGluIleAlaSer 180185190 LysGlnValGluGluArgLeuGlnGluGluLysSerGlnLysGlnAsn 195200205 IleAspIleAsnArgGlnAlaLysPheAlaAlaThrProSerLeuAla 210215220 LeuPheValAsnLeuLysAsnValValCysLysIleGlyGluAspAla 225230235240 GluValLeuMetSerLeuTyrAspProValGluSerLysPheIleSer 245250255 GluAsnTyrLeuValArgTrpSerSerSerGlyLeuProLysAspIle 260265270 AspArgLeuHisAsnLeuArgAlaValPheThrAspLeuGlySerLys 275280285 AspLeuLysArgGluLysIleSerPheValCysGlnIleValArgVal 290295300 GlyArgMetGluLeuArgAspAsnAsnThrArgLysLeuThrSerGly 305310315320 LeuArgArgProPheGlyValAlaValMetAspValThrAspIleIle 325330335 AsnGlyLysValAspAspGluAspLysGlnHisPheIleProPheGln 340345350 ProValAlaGlyGluAsnAspPheLeuGlnThrValIleAsnLysVal 355360365 IleAlaAlaLysGluValAsnHisLysGlyGlnGlyLeuTrpValThr 370375380 LeuLysLeuLeuProGlyAspIleHisGlnIleArgLysGluPhePro 385390395400 HisLeuValAspArgThrThrAlaValAlaArgLysThrGlyPhePro 405410415 GluIleIleMetProGlyAspValArgAsnAspIleTyrValThrLeu 420425430 ValGlnGlyAspPheAspLysGlySerLysThrThrAlaLysAsnVal 435440445 GluValThrValSerValTyrAspGluAspGlyLysArgLeuGluHis 450455460 ValIlePheProGlyAlaGlyAspGluAlaIleSerGluTyrLysSer 465470475480 ValIleTyrTyrGlnValLysGlnProArgTrpPheGluThrValLys 485490495 ValAlaIleProIleGluAspValAsnArgSerHisLeuArgPheThr 500505510 PheArgHisArgSerSerGlnAspSerLysAspLysSerGluLysIle 515520525 PheAlaLeuAlaPheValLysLeuMetArgTyrAspGlyThrThrLeu 530535540 ArgAspGlyGluHisAspLeuIleValTyrLysAlaGluAlaLysLys 545550555560 LeuGluAspAlaAlaThrTyrLeuSerLeuProSerThrLysAlaGlu 565570575 LeuGluGluLysGlyHisSerAlaThrGlyLysSerMetGlnSerLeu 580585590 GlySerCysThrIleSerLysAspSerPheGlnIleSerThrLeuVal 595600605 CysSerThrLysLeuThrGlnAsnValAspLeuLeuGlyLeuLeuLys 610615620 TrpArgSerAsnThrSerLeuLeuGlnGlnAsnLeuArgGlnLeuMet 625630635640 LysValAspGlyGlyGluValValLysPheLeuGlnAspThrLeuAsp 645650655 AlaLeuPheAsnIleMetMetGluAsnSerGluSerGluThrPheAsp 660665670 ThrLeuValPheAspAlaLeuValPheIleIleGlyLeuIleAlaAsp 675680685 ArgLysPheGlnHisPheAsnProValLeuGluThrTyrIleLysLys 690695700 HisPheSerAlaThrLeuAlaTyrThrLysLeuThrLysValLeuLys 705710715720 AsnTyrValAspGlyAlaGluLysProGlyValAsnGluGlnLeuTyr 725730735 LysAlaMetLysAlaLeuGluSerIlePheLysPheIleValArgSer 740745750 ArgIleLeuPheAsnGlnLeuTyrGluAsnLysGlyGluAlaAspPhe 755760765 ValGluSerLeuLeuGlnLeuPheArgSerIleAsnAspMetMetSer 770775780 SerMetSerAspGlnThrValArgValLysGlyAlaAlaLeuLysTyr 785790795800 LeuProThrIleValAsnAspValLysLeuValPheAspProLysGlu 805810815 LeuSerLysMetPheThrGluPheIleLeuAsnValProMetGlyLeu 820825830 LeuThrIleGlnLysLeuTyrCysLeuIleGluIleValHisSerAsp 835840845 LeuPheThrGlnHisAspCysArgGluIleLeuLeuProMetMetThr 850855860 AspGlnLeuLysTyrHisLeuGluArgGlnGluAspLeuGluAlaCys 865870875880 CysGlnLeuLeuSerHisIleLeuGluValLeuTyrArgLysAspVal 885890895 GlyProThrGlnArgHisValGlnIleIleMetGluLysLeuLeuArg 900905910 ThrValAsnArgThrValIleSerMetGlyArgAspSerGluLeuIle 915920925 GlyAsnPheValAlaCysMetThrAlaIleLeuArgGlnMetGluAsp 930935940 TyrHisTyrAlaHisLeuIleLysThrPheGlyLysMetArgThrAsp 945950955960 ValValAspPheLeuMetGluThrPheIleMetPheLysAsnLeuIle 965970975 GlyLysAsnValTyrProPheAspTrpValIleMetAsnMetValGln 980985990 AsnLysValPheLeuArgAlaIleAsnGlnTyrAlaAspMetLeuAsn 99510001005 LysLysPheLeuAspGlnAlaAsnPheGluLeuGlnLeuTrpAsnAsn 101010151020 TyrPheHisLeuAlaValAlaPheLeuThrGlnGluSerLeuGlnLeu 1025103010351040 GluAsnPheSerSerAlaLysArgAlaLysIleLeuAsnLysTyrGly 104510501055 AspMetArgArgGlnIleGlyPheGluIleArgAspMetTrpTyrAsn 106010651070 LeuGlyGlnHisLysIleLysPheIleProGluMetValGlyProIle 107510801085 LeuGluMetThrLeuIleProGluThrGluLeuArgLysAlaThrIle 109010951100 ProIlePhePheAspMetMetGlnCysGluPheHisSerThrArgSer 1105111011151120 PheGlnMetPheGluAsnGluIleIleThrLysLeuAspHisGluVal 112511301135 GluGlyGlyArgGlyAspGluGlnTyrLysValLeuPheAspLysIle 114011451150 LeuLeuGluHisCysArgLysHisLysTyrLeuAlaLysThrGlyGlu 115511601165 ThrPheValLysLeuValValArgLeuMetGluArgLeuLeuAspTyr 117011751180 ArgThrIleMetHisAspGluAsnLysGluAsnArgMetSerCysThr 1185119011951200 ValAsnValLeuAsnPheTyrLysGluIleGluArgGluGluMetTyr 120512101215 IleArgTyrLeuTyrLysLeuCysAspLeuHisLysGluCysAspAsn 122012251230 TyrThrGluAlaAlaTyrThrLeuLeuLeuHisAlaLysLeuLeuLys 123512401245 TrpSerGluAspValCysValAlaHisLeuThrGlnArgAspGlyTyr 125012551260 GlnAlaThrThrGlnGlyGlnLeuLysGluGlnLeuTyrGlnGluIle 1265127012751280 IleHisTyrPheAspLysGlyLysMetTrpGluGluAlaIleAlaLeu 128512901295 GlyLysGluLeuAlaGluGlnTyrGluAsnGluMetPheAspTyrGlu 130013051310 GlnLeuSerGluLeuLeuLysLysGlnAlaGlnPheTyrGluAsnIle 131513201325 ValLysValIleArgProLysProAspTyrPheAlaValGlyTyrTyr 133013351340 GlyGlnGlyPheProThrPheLeuArgGlyLysValPheIleTyrArg 1345135013551360 GlyLysGluTyrGluProArgGluAspPheGluAlaArgLeuLeuThr 136513701375 GlnPheProAsnAlaGluLysMetLysThrThrSerProProGlyAsp 138013851390 AspIleLysAsnSerProGlyGlnTyrIleGlnCysPheThrValLys 139514001405 ProLysLeuAspLeuProProLysPheHisArgProValSerGluGln 141014151420 IleValSerPheTyrArgValAsnGluValGlnArgPheGluTyrSer 1425143014351440 ArgProIleArgLysGlyGluLysAsnProAspAsnGluPheAlaAsn 144514501455 MetTrpIleGluArgThrIleTyrThrThrAlaTyrLysLeuProGly 146014651470 IleLeuArgTrpPheGluValLysSerValPheMetValGluIleSer 147514801485 ProLeuGluAsnAlaIleGluThrMetGlnLeuThrAsnAspLysIle 149014951500 AsnSerMetValGlnGlnHisLeuAspAspProSerLeuProIleAsn 1505151015151520 ProLeuSerMetLeuLeuAsnGlyIleValAspProAlaValMetGly 152515301535 GlyPheAlaAsnTyrGluLysAlaPhePheThrAspArgTyrLeuGln 154015451550 GluHisProGluAlaHisGluLysIleGluLysLeuLysAspLeuIle 155515601565 AlaTrpGlnIleProPheLeuAlaGluGlyIleArgIleHisGlyAsp 157015751580 LysValThrGluAlaLeuArgProPheHisGluArgMetGluAlaCys 1585159015951600 PheLysGlnLeuLysGluLysValGluLysGluTyrGlyValArgIle 160516101615 MetProSerSerLeuAspAspArgArgGlySerArgProArgSerMet 162016251630 ValArgSerPheThrMetProSerSerSerArgProLeuSerValAla 163516401645 SerValSerSerLeuSerSerAspSerThrProSerArgProGlySer 165016551660 AspGlyPheAlaLeuGluProLeuLeuProLysLysMetHisSerArg 1665167016751680 SerGlnAspLysLeuAspLysAspAspLeuGluLysGluLysLysAsp 168516901695 LysLysLysGluLysArgAsnSerLysHisGlnGluIlePheGluLys 170017051710 GluPheLysProThrAspIleSerLeuGlnGlnSerGluAlaValIle 171517201725 LeuSerGluThrIleSerProLeuArgProGlnArgProLysSerGln 173017351740 ValMetAsnValIleGlySerGluArgArgPheSerValSerProSer 1745175017551760 SerProSerSerGlnGlnThrProProProValThrProArgAlaLys 176517701775 LeuSerPheSerMetGlnSerSerLeuGluLeuAsnGlyMetThrGly 178017851790 AlaAspValAlaAspValProProProLeuProLeuLysGlySerVal 179518001805 AlaAspTyrGlyAsnLeuMetGluAsnGlnAspLeuLeuGlySerPro 181018151820 ThrProProProProProProHisGlnArgHisLeuProProProLeu 1825183018351840 ProSerLysThrProProProProProProLysThrThrArgLysGln 184518501855 ThrSerValAspSerGlyIleValGln 18601865 __________________________________________________________________________
Claims
1. A cDNA of a DOCK180 gene which encodes a DOCK180 protein having the amino acid sequence according to SEQ ID NO: 2.
2. A cDNA of a DOCK180 gene, which has a nucleotide sequence according to SEQ ID No: 1. and whose translation product binds to proto-oncogene product CRK.
3. A recombinant vector containing the cDNA as claimed in claim 2.
4. Plasmid pDOCK180, which is inserted in E. coli DOCK180 (FERM BP-5362).
5. A purified DOCK180 protein having an amino acid sequence according to SEQ ID NO: 2.
6. A DOCK180 protein having an amino acid sequence according to SEQ ID NO: 2, which is expressed from the cDNA of the DOCK180 gene claimed in claim 2.
- Hasegawa et al. (1996) 16:1770-1776. Matsuda et al. (1996) 271:14468-14472.
Type: Grant
Filed: Jan 19, 1996
Date of Patent: Jul 7, 1998
Assignee: Research Development Corporation of Japan (Saitama)
Inventors: Michiyuki Matsuda (Tokyo), Takeshi Kurata (Tokyo)
Primary Examiner: John Ulm
Assistant Examiner: Kenneth A. Sorensen
Law Firm: Wenderoth, Lind & Ponack
Application Number: 8/588,985
International Classification: C12N 1512;